rs1057517799

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs1057517799(G;T)

Make rs1057517799(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

22247940

Gene	PHEX, PTCHD1-AS

is a	snp
is	mentioned by
dbSNP	rs1057517799
dbSNP (classic)	rs1057517799
ClinGen	rs1057517799
ebi	rs1057517799
HLI	rs1057517799
Exac	rs1057517799
Gnomad	rs1057517799
Varsome	rs1057517799
LitVar	rs1057517799
Map	rs1057517799
PheGenI	rs1057517799
Biobank	rs1057517799
1000 genomes	rs1057517799
hgdp	rs1057517799
ensembl	rs1057517799
geneview	rs1057517799
scholar	rs1057517799
google	rs1057517799
pharmgkb	rs1057517799
gwascentral	rs1057517799
openSNP	rs1057517799
23andMe	rs1057517799
SNPshot	rs1057517799
SNPdbe	rs1057517799
MSV3d	rs1057517799
GWAS Ctlg	rs1057517799

Max Magnitude

0

ClinVar
Risk	rs1057517799(T;T)
Alt	rs1057517799(T;T)
Reference	Rs1057517799(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	PTCHD1-AS PHEX
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.22266057G>T
CLNSRC
CLNACC	RCV000413405.1,